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  2. Villitis of unknown etiology - Wikipedia

    en.wikipedia.org/wiki/Villitis_of_unknown_etiology

    High grade chronic villitis has more than 10 inflamed villi per focus. High grade chronic villitis is differentiated into diffuse and patchy. The term patchy is used if less than 30% of distal villi are involved. The term diffuse is used if more than 30% of distal villi are involved. [citation needed] VUE has 2 prominent distinct patterns.

  3. ICD coding for rare diseases - Wikipedia

    en.wikipedia.org/wiki/ICD_coding_for_rare_diseases

    Europe and other parts of the world use the ICD-10. The root codes for ICD-10 and ICD-10-CM are the same, making it helpful for locating codes for general body systems and disease processes. [2] [3] In ICD-11 the search and coding of any disease, including rare ones is done via the ICD-11 website. [4]

  4. Microvillous inclusion disease - Wikipedia

    en.wikipedia.org/wiki/Microvillous_inclusion_disease

    One patient from the UK was documented as achieving nutritional independence at age 3. [10] On 26 June 2009, a six-year-old girl with microvillus inclusion disease became the third person in the UK to die of swine flu. This was attributed to her weakened immune system. [11]

  5. Extravillous trophoblast - Wikipedia

    en.wikipedia.org/wiki/Extravillous_trophoblast

    Extravillous trophoblasts (EVTs), are one form of differentiated trophoblast cells of the placenta.They are invasive mesenchymal cells which function to establish critical tissue connection in the developing placental-uterine interface.

  6. Placental villous immaturity - Wikipedia

    en.wikipedia.org/wiki/Placental_villous_immaturity

    Placental villous immaturity is chorionic villous development that is inappropriate for the gestational age. It is associated with diabetes mellitus [ 1 ] and fetal death near term, i.e. intrauterine demise close to the normal gestational period .

  7. L1 syndrome - Wikipedia

    en.wikipedia.org/wiki/L1_syndrome

    L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS).

  8. Potter sequence - Wikipedia

    en.wikipedia.org/wiki/Potter_sequence

    It includes clubbed feet, pulmonary hypoplasia and cranial anomalies related to the oligohydramnios. [clarification needed] Oligohydramnios is the decrease in amniotic fluid volume sufficient to cause deformations in morphogenesis of the baby. Oligohydramnios is the cause of Potter sequence, but there are many things that can lead to ...

  9. Benign lymphoepithelial lesion - Wikipedia

    en.wikipedia.org/wiki/Benign_lymphoepithelial_lesion

    Historically, bilateral parotid and lacrimal gland enlargement was characterized by the term Mikulicz's disease if the enlargement appeared apart from other diseases. If it was secondary to another disease, such as tuberculosis, sarcoidosis, lymphoma, and Sjögren's syndrome, the term used was Mikulicz's syndrome.